首页> 外国专利> methods of identifying a genetic variant that is associated with the development of a condition of interest and a patient in a clinical trial of a treatment for alzheimer's disease, of determining increasing risks of developing a condition of interest, alzheimer's disease in a patient , a prognosis, or the risk of developing alzheimer's disease in a patient, treating a patient for alzheimer's disease, a condition of interest and alzheimer's disease in a patient, stratifying a patient into a subgroup of a clinical trial of a therapy for the treatment of alzheimer's disease, use of an active anti-alzheimer's disease agent, and kits to determine if a patient is at increased risk of developing alzheimer's disease and if a patient is responsive to treatment for a condition of interest

methods of identifying a genetic variant that is associated with the development of a condition of interest and a patient in a clinical trial of a treatment for alzheimer's disease, of determining increasing risks of developing a condition of interest, alzheimer's disease in a patient , a prognosis, or the risk of developing alzheimer's disease in a patient, treating a patient for alzheimer's disease, a condition of interest and alzheimer's disease in a patient, stratifying a patient into a subgroup of a clinical trial of a therapy for the treatment of alzheimer's disease, use of an active anti-alzheimer's disease agent, and kits to determine if a patient is at increased risk of developing alzheimer's disease and if a patient is responsive to treatment for a condition of interest

机译:在阿尔茨海默氏病治疗的临床试验中鉴定与目标疾病和患者发展相关的遗传变异的方法,确定在患者中发展目标疾病阿尔茨海默氏病的风险,以及预后,或在患者中罹患阿尔茨海默氏病的风险,在患者中治疗阿尔茨海默氏病,所关注的疾病和阿尔茨海默氏病的风险,将患者分为治疗阿尔茨海默氏病的临床试验的亚组,活性抗阿尔茨海默氏病药物的使用和试剂盒,以确定患者是否罹患阿尔茨海默氏病的风险增加,以及患者是否对所关注疾病的治疗有反应

摘要

Provided herein is a method for identifying a genetic variant that is associated with development of a condition of interest (e.g., Alzheimer's disease), and genetic variants so identified. Methods of treatment with an active agent (e.g., with a particular active agent and/or at an earlier age) is also provided, upon detecting a genetic variant described herein. In some embodiments, the genetic variant is a deletion/insertion polymorphism (DIP) of the TOMM40 gene. Kits for determining if a subject is at increased risk of developing late onset Alzheimer's disease is also provided. Kits for determining if a subject is responsive to treatment for a condition of interest with an active agent are further provided..
机译:本文提供了一种鉴定与目的疾病(例如阿尔茨海默氏病)的发展相关的遗传变异的方法,以及由此鉴定的遗传变异。当检测到本文所述的遗传变异时,还提供了用活性剂(例如,用特定的活性剂和/或处于较早年龄)治疗的方法。在一些实施方案中,遗传变异体是TOMM40基因的缺失/插入多态性(DIP)。还提供了用于确定受试者是否具有发展为迟发性早老性阿尔茨海默氏病的风险的试剂盒。还提供了用于确定受试者是否对用活性剂治疗感兴趣的病症有反应的试剂盒。

著录项

  • 公开/公告号BRPI0917948A2

    专利类型

  • 公开/公告日2017-06-20

    原文格式PDF

  • 申请/专利权人 ZINFANDEL PHARRMACEUTICALS INC.;

    申请/专利号BR2009PI17948

  • 发明设计人 ALLEN D. ROSES;

    申请日2009-08-11

  • 分类号G01N33/48;G01N33/50;

  • 国家 BR

  • 入库时间 2022-08-21 13:39:42

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